Regulatory Affairs Consultant, Biosimilars

🕒 March 17

🇺🇸 United States – Remote

⏳ Contract/Temporary

🟠 Senior

🔴 Lead

🚔 Compliance

👻 Ghost score 44%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Pharmavise Corporation

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2013

💼 Consulting

📦 Logistics

🏭 Manufacturing

Consulting • Logistics • Manufacturing

Pharmavise Corporation is the first Continuous Compliance Organization (CCO) dedicated to maintaining the highest standards of quality and regulatory compliance in the life sciences industry. Our esteemed client base includes Fortune 500 companies in pharmaceuticals, medical devices, and biotechnology. We offer bespoke solutions tailored to meet the specific compliance needs of our clients, supporting them from development through commercialization and ensuring they exceed their compliance goals while enhancing patient health and safety.

📋 Description

• Provide expert regulatory affairs guidance and support for biosimilars development projects. • Review and analyze regulatory requirements and guidelines related to biosimilars in various regions. • Assist in the preparation, submission, and maintenance of regulatory submissions for biosimilars, including INDs, BLAs, and variations. • Collaborate with cross-functional teams to ensure alignment on regulatory strategy and objectives. • Stay updated on regulatory developments and trends impacting biosimilars globally. • Participate in meetings with regulatory authorities as needed. • Provide regulatory support and expertise during regulatory agency inspections and audits.

🎯 Requirements

• Bachelor's degree in a scientific or related field; advanced degree preferred. • Minimum of 8 years of experience in regulatory affairs within the pharmaceutical or biotechnology industry, with specific expertise in biosimilars preferred. • Strong understanding of regulatory requirements and guidelines governing biosimilars development and approval processes. • Experience with regulatory submissions for biosimilars, including INDs, BLAs, and variations. • Excellent communication and interpersonal skills, with the ability to effectively collaborate with internal and external stakeholders. • Proven ability to work independently and manage multiple projects simultaneously. • Regulatory affairs certification (RAC) preferred but not required.

🏖️ Benefits

• Competitive compensation packages are available